Stabilized synthetic polymers

ABSTRACT

Esters of 2,2,6,6-tetramethylpiperidinols with mono- or bis-hydroxybenzylmalonic acids are powerful stabilizers for organic polymers, especially for polyolefins. They protect the polymers against thermal-oxidative degradation as well as against light-induced aging. Similar activity show the corresponding amides of hydroxybenzylmalonic acids. The esters and the amides can be prepared by analogous processes.

This is a continuation of application Ser. No. 744,352 filed on Nov. 23,1976 now abandoned, which latter application is a divisional ofapplication Ser. No. 525,810, filed on Nov. 21, 1974, now U.S. Pat. No.3,993,655.

The invention relates to new derivatives of hydroxybenzylmalonic acids,to their preparation, and to their use as stabilisers for syntheticpolymers, as well as to the material stabilised with the aid of the saidderivatives.

The compounds concerned are those of formula (I) ##STR1## wherein

X can be oxygen or --NH--,

Y represents hydrogen, the radical --O., an alkyl group having 1 to 12carbon atoms, an alkenyl group having 3 or 4 carbon atoms, a propargylgroup, a benzyl group, or a group of the formula ##STR2## wherein R₆represents hydrogen, methyl or phenyl, and R₇ represents hydrogen, or anacyl group having up to 18 carbon atoms,

R₁ represents a hydroxybenzyl group of formula (II) ##STR3## wherein R₃and R₄ each independently represent an alkyl group having 1 to 8 carbonatoms, and

R₅ represents hydrogen or methyl, and

R₂ represents, if X is oxygen, hydrogen or a hydroxybenzyl group offormula (II); if, however, X is --NH--, only hydrogen.

In the case where Y denotes an alkyl group, it can be a primary alkylgroup, such as, e.g. a methyl, ethyl, n-propyl, n-butyl, n-hexyl,n-octyl, n-decyl or n-dodecyl group.

The symbols R₃ and R₄ can have the same meaning as R, but in additionrepresent a secondary or tertiary alkyl group, such as, e.g. aisopropyl, sec.butyl, 2-ethylhexyl, tert.butyl or tert.octyl group.

Where Y represents an alkenyl group, it can be, for example, an allyl ormethallyl group. As an acyl group, R₇ can be an aliphatic acyl group,for example, an acetyl, propionyl, hexanoyl, acryl, methacryl,2-ethyl-hexanoyl, dodecanoyl or octadecanoyl group, and also an aromaticacyl group, especially a benzoyl group.

These compounds impart to synthetic polymers excellent protection bothagainst thermal-oxidative ageing and against light-induced ageing. As isknown, organic polymers are slowly decomposed both by light and byoxygen, a factor which leads to a gradual falling off of the performanceproperties. This ageing is further accelerated by heat; on the otherhand, it can be greatly retarded by the addition of stabilisers. It isknown that hydroxybenzylmalonic acid derivatives can be used asanti-oxidative stabilisers for polymers; however, such compounds arecompletely lacking with regard to protective action against the effectsof light rays. In this respect, however, it is also known thatderivatives of 2,2,6,6-tetramethylpiperidine do act as lightstabilisers, but on their own exhibit no perceptible antioxidativeaction. The said new compounds of formula I constitute a molecularcombination of these two structures. Compared with a mixture of ananti-oxidant of the hydroxybenzylmalonic acid series and a lightstabiliser of the tetramethylpiperidine series, the new compounds havethe advantage of a more simple incorporation and of an overall uniformlyconstant ratio of anti-oxidant to light stabiliser. Surprisingly,however, there has been found yet another advantage; these new compoundshave a greater stabilising action than that of the same amount of amixture of a hydroxybenzylmalonic acid derivative and atetramethylpiperidine derivative. This means in practice that the sameeffect can be obtained with a smaller amount of stabiliser.

Two classes are preferred among the compounds of formula (I): the oneclass is formed by the para-hydroxybenzyl compounds such as thosecorresponding to formula (I) where R₁ represents a group of formula(IIa) ##STR4## wherein R₃ denotes an isopropyl, tert.butyl or tert.amylgroup, and R₄ denotes a methyl, ethyl, isopropyl, tert.butyl, tert.amylor tert.octyl group, and where Y in formula (I) represents hydrogen, theradical --O. or a methyl, allyl or benzyl group.

Particularly preferred compounds among these are those in which R₃represents a tertiary butyl group, R₄ represents a methyl or tert.butylgroup, R₅ represents hydrogen, and Y hydrogen, the radical --O. or amethyl group.

The other class of preferred substances is the meta-hydroxybenzylcompounds. These correspond to formula (I) where R₁ represents a groupof formula (IIb) ##STR5## wherein R₃ denotes a tert.butyl, tert.amyl ortert.octyl group, and Y represents hydrogen, the radical --O. or amethyl group.

Examples of compounds of the first mentioned class are:

bis(3,5-di-tert.butyl-4-hydroxybenzyl)malonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester,

bis(3,5-di-isopropyl-4-hydroxybenzyl)malonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester,

bis(3-tert.butyl-4-hydroxy-5-methylbenzyl)malonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl-1-oxyl)ester,

3,5-di-tert.butyl-4-hydroxybenzylmalonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl-1-oxyl)ester,

3-tert.butyl-4-hydroxy-5,6-dimethylbenzylmalonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester

3-tert.butyl-4-hydroxy-5,6-dimethylbenzylmalonicacid-bis(1,2,2,6,6-pentamethyl-4-piperidinyl)ester,

bis(3-tert.butyl-4-hydroxy-5,6-dimethylbenzyl)malonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester,

bis(3-tert.butyl-4-hydroxy-5,6-dimethylbenzyl)malonicacid-bis(1,2,2,6,6-pentamethyl-4-piperidinyl)ester,

3-tert.butyl-4-hydroxy-5,6-dimethylbenzylmalonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl-1-oxyl)ester,

3-tert.butyl-4-hydroxy-5,6-dimethylbenzylmalonicacid-N,N'-bis-(2,2,6,6-tetramethyl-4-piperidinyl)amide,

bis-(3,5-di-tert.butyl-4-hydroxybenzyl)malonicacid-bis(1-octyl-2,2,6,6-tetramethyl-4-piperidinyl)ester,

3-tert.butyl-4-hydroxy-5,6-dimethylbenzylmalonicacid-bis(1-allyl-2,2,6,6-tetramethyl-4-piperidinyl)ester,

3,5-di-tert.butyl-4-hydroxybenzylmalonicacid-N,N'-bis-(2,2,6,6-tetramethyl-4-piperidinyl)-N,N'-dimethylamide,

3,5-di-tert.butyl-4-hydroxybenzylmalonicacid-bis-[1(2'-hydroxyethyl)2,2,6,6-tetramethyl-4-piperidinyl]ester.

Examples of compounds of the second-mentioned class are:

4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonicacid-bis-(2,2,6,6-tetramethyl-4-piperidinyl)ester,

bis(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)malonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester,

4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonicacid-bis-(2,2,6,6-pentamethyl-4-piperidinyl)ester,

bis(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)malonicacid-bis(1,2,2,6,6-pentamethyl-4-piperidinyl)ester,

4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonicacid-bis-(2,2,6,6-tetramethyl-4-piperidinyl)ester,

4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonicacid-N-(1,2,2,6,6-pentamethyl-4-piperidinyl)amide,

bis(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)malonicacid-bis(1-allyl-2,2,6,6-tetramethyl-4-piperidinyl)ester,

4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonicacid-bis-(1-propargyl-2,2,6,6-tetramethyl-4-piperidinyl)ester,

4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonicacid-bis[1(2'-acetoxyethyl)2,2,6,6-tetramethyl-4-piperidinyl]ester.

The compounds of formula (I) can be prepared by various processes. Themost important process comprises the reaction of a malonic acidderivative of formula (III) ##STR6## with, if X is oxygen, one mole ortwo moles, and, if X is --NH--, with one mole, of anN-dialkyldithiocarbaminate of formula (IV) ##STR7## or of ahydroxybenzylamine of formula (V) ##STR8## in the presence of a basiccatalyst, whereby in the above formulae

X can be oxygen or --NH--,

Y represents hydrogen, the radical --O., an alkyl group having 1 to 12carbon atoms, an alkenyl group having 3 or 4 carbon atoms, a propargylgroup, a benzyl group, or a group of the formula ##STR9## wherein

R₆ represents hydrogen, methyl or phenyl, and R₇ represents hydrogen, oran acyl group having up to 18 carbon atoms,

R₁ represents a hydroxybenzyl group of formula (II) ##STR10## wherein R₃and R₄ each independently represent an alkyl group having 1 to 8 carbonatoms, and

R₅ represents hydrogen or methyl, and

R₈ represents an alkyl group having 1 to 5 carbon atoms, or the tworadicals R₈ together with the N-atom represent a morpholine, piperidineor pyrrolidine ring.

The starting substances of formula (III) are malonic acid esters andmalonic acid amides of 4-hydroxy- and 4-aminotetramethylpiperidines,respectively. They are obtainable by standard processes; for example, bybase-catalysed transesterification of diethylmalonate with 2 moles of a4-hydroxy- or 4-aminotetramethylpiperidine. The compounds of formula(IV) are obtainable by reaction of a phenol of the formula R₁ --H withformaldehyde, carbon disulphide and a secondary amine (R₈)₂ NH.

The reaction of the components (III) and (IV) in the case of the esters(X=O) can be performed in the molar ratio of 1:1 or 1:2. In the firstcase are obtained the monohydroxybenzyl compounds of formula (I) whereinR₂ =H, and in the second case the di-hydroxybenzyl compounds of formula(I) wherein R₂ =R₁. With regard to the amides (X=--NH--), the reactionceases, even with use of more than 1 mole (IV), at the first stage, sothat here there are obtained only the final products wherein R₂ =H.Suitable basic catalysts are, for example, alkali hydroxides such asNaOH or KOH, alkali or alkaline-earth alcoholates such as CH₃ ONa, C₂ H₅ONa, (CH₃)₃ COK, (C₂ H₅ O)₂ Mg or (CH₃)₂ CHOLi, alkali hydrides oralkaline-earth hydrides such as LiH, NaH or CaH₂, and alkali amides suchas NaNH₂, LiNH₂ or KNH₂. Those preferably used are alkali hydroxides.These bases are preferably employed in equimolar amounts, i.e. per moleof dithiocarbaminate is used one mole-equivalent of the base. Thereaction can be performed in solution; this method ensures bettertemperature control, and is to be particularly recommended withhigh-melting starting components. Suitable solvents are, for example,alcohols, such as methanol, ethanol, isopropanol or tert.butanol; alsosuitable are aliphatic ethers or cyclic ethers, such as diethyl ether,tetrahydrofuran or dioxane; also hydrocarbons such as hexane, heptane,ligroin, decalin, cyclohexane, benzene, toluene or xylene, as well aspolar aprotic solvents, such as dimethylformamide, dimethylacetamide ordimethylsulphoxide. The last-mentioned group of solvents is torecommended, in particular, with use of the malonamide of formula (II),X=NH.

Instead of using dithiocarbaminates, it is possible to use thecorresponding hydroxybenzylamines of formula (V). In this case too, thereaction can be performed with or without solvents, whereby likewise theabove-mentioned solvents are suitable. And also with respect tocatalysts, the same basic substances as described above are applicable.It is preferable to use alkali amides and alkali alcoholates. They areapplied in catalytic amounts, i.e. approximately in amounts of 0.1 to 5Mol-%. Use of larger amounts of the base is of no advantage.

A further process for the preparation of compounds of formula (I)consists in the reaction of a malonic acid dialkyl ester of formula (VI)with two moles of a tetramethylpiperidine derivative of formula (VII):##STR11## The symbol R₉ in the formula represents an alkyl radicalhaving 1 to 4 carbon atoms. Suitable bases as catalysts are the same asthose described previously. In this process too, the reaction can beperformed in a solvent, whereby, with the exception of the alcohols, allthe previously mentioned groups of solvents are suitable.

In all the processes discussed here, the reaction is normally performedat elevated temperature, in order to ensure a rapid and complete courseof reaction. Isolation of the products can be carried out by the usualmethods, for example, by concentration through evaporation, andcrystallisation of the residue. It is advantageous for the base to beneutralised before the solvent is distilled off.

According to the present invention, the compounds of formula (I) can beused as stabilisers for organic polymers. Such organic polymers are, forexample:

1. Polymers which are derived from hydrocarbons with single or doubleunsaturation, e.g. polyolefins such as polyethylene, which can beoptionally cross-linked, polypropylene, polybutene-1, polyisobutene,polymethylbutene-1, polymethylpentene-1, polyisoprene, polybutadiene,polystyrene, copolymers of the monomers on which the mentionedhomopolymers are based, such as ethylenepropylene copolymers,propylene-butene-1 copolymers, propylene-isobutene copolymers,styrene-butadiene copolymers, as well as terpolymers of ethylene andpropylene with a diene, such as, e.g. hexadiene, dicyclopentadiene orethylidenenorbornene; mixtures of the above given homopolymers, such as,for example, mixtures of polypropylene and polyethylene, polypropyleneand polybutene-1, polypropylene and polyisobutylene, or ofbutadiene-acrylonitrile copolymerisate with a styrene-butadienecopolymerisate.

2. Halogen-containing vinylpolymers, such as polyvinyl chloride,polyvinylidene chloride, polyvinylfluoride, polychloroprene andchlorinated rubbers.

3. Polymers derived from α,β-unsaturated acids and their derivatives,such as polyacrylates and polymethacrylates, polyacrylamides andpolyacrylnitrile, as well as copolymers with other vinyl compounds, suchas acrylonitrile/butadiene/styrene, acrylonitrile/styrene andacrylonitrile/styrene/acrylic ester copolymers.

4. Polymers derived from unsaturated alcohols and amines or their acylderivatives or acetals, such as polyvinyl alcohol, polyvinyl acetate,polyvinyl stearate, polyvinyl benzoate, polyvinyl maleate, polyvinylbutyral, polyallyl phthalate, polyallyl melamine and their copolymerswith other vinyl compounds, such as ethylene/vinyl acetate copolymers.

5. Homopolymers and copolymers derived from epoxides, such aspolyethylene oxide, or the polymerisates which are derived frombis-glycidyl ethers.

6. Polyacetals, such as polyoxymethylene and polyoxyethylene, as well asthose polyoxymethylenes which contain ethylene oxide as the comonomer.

7. Polyphenylene oxides.

8. Polyurethanes and polyureas.

9. Polycarbonates.

10. Polysulphones.

11. Polyamides and copolyamides derived from diamines and dicarboxylicacids and/or from aminocarboxylic acids or the corresponding lactams,such as polyamide 6, polyamide 6/6, polyamide 6/10, polyamide 11 andpolyamide 12.

12. Polyesters derived from dicarboxylic acids and dialcohols and/orfrom hydroxycarboxylic acids or the corresponding lactones, such aspolyethylene glycol terephthalate, polybutylene terephthalate,poly-1,4-dimethylol-cyclohexane terephthalate, as well as their startingmaterials, such as lower terephthalic acid alkyl esters.

13. Cross-linked polymerisates which are derived from aldehydes on theone hand, and from phenols, ureas and melamines on the other, such asphenol-formaldehyde resins, urea-formaldehyde resins andmelamine-formaldehyde resins.

14. Alkyd resins, such as glycerin-phthalic acid resins and mixturesthereof with melamine-formaldehyde resins.

15. Unsaturated polyester resins derived from copolyesters of saturatedand unsaturated dicarboxylic acids with polyvalent alcohols, as well asvinyl compounds as cross-linking agents, and also theirhalogen-containing, difficulty combustible modifications.

16. Natural polymers, such as cellulose, rubber and proteins, as well astheir polymer-homologously chemically modified derivatives, such ascellulose acetates, cellulose propionates and cellulose butyrates, orcellulose ethers, such as methylcellulose.

Preferred polymers are polyethylene of high and low density,polypropylene, polybutadiene, polyurethanes, polystyrene and itscopolymers, as well as mixtures thereof.

The new compounds are added to the substrates in a concentration of 0.01to 5 percent by weight, calculated on the material to be stabilised.Preferably, 0.05 to 1.5, particularly preferably 0.1 to 0.8, percent byweight of the compounds, calculated on the material to be stabilised, isincorporated into the said material.

Incorporation can be effected after polymerisation; for example, by themixing of the compounds and, optionally, further additives into themelt, by methods common in practice, before or during moulding(shaping); or by application of the dissolved or dispersed compounds tothe polymers, optionally with subsequent removal of the solvent byevaporation.

The new compounds can also be added in the form of a master batch,containing these compounds in a concentration of, for example, 2.5 to 25percent by weight, to the polymers to be stabilised.

In the case of cross-linked polyethylene, the compounds are added beforecross-linking.

In addition to the compounds of formula (I), other known stabilisers maybe added to the polymers, or other additives commonly used in plasticstechnology, such as, e.g. flame-retarding agents, antistatic agents,plasticisers, lubricants, expanding agents, pigments or fillers.

The preparation and use of the compounds according to the invention isfurther illustrated in the following examples. The term `parts` denotesparts by weight and % percent by weight; temperatures are expressed indegrees Centigrade.

EXAMPLE 1

12.3 g (0.03 mole) of bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)malonateand 19.5 g (0.06 mole) ofN-diethyl-S-(3-methyl-5-tert.-butyl-4-hydroxybenzyl)dithiocarbaminateare dissolved in 100 ml of isopropanol. An addition is made dropwise at60° in the course of 15 minutes, with stirring, of 2.4 g of NaOH (0.06mole) in 12 ml of water. The whole is subsequently refluxed for 2 hoursand then cooled to 50°; an amount of 72 ml of 1% acetic acid is addedand the mixture cooled to 0°. The product thereupon crystallises out andis recrystallised from ligroin to thus obtain 18.7 g (85.7% of theory)of bis-(3-methyl-5-tert.butyl-4-hydroxybenzyl)malonicacid-bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)ester, M.P. 150°.

EXAMPLES 2 to 5

As described in Example 1, 1 mole of a malonic acid ester of formula(IIIa) is in each case reacted with two moles of anN-diethyldithiocarbaminate of formula (IVa) and two moles of sodiumhydroxide solution, with the products listed in the following Table 1being obtained. ##STR12##

                  TABLE I                                                         ______________________________________                                        Test                                                                          No.  Y        R.sub.3  Product         M.P.                                   ______________________________________                                        2    CH.sub.3 t-C.sub.4 H.sub.9                                                                      bis(3,5-di-tert.butyl-                                                                        239° C.                                                4-hydroxybenzyl)malonic                                                       acid-bis(1,2,2,6,6-                                                           pentamethyl-4-piperidi-                                                       nyl)ester                                              3    H        CH.sub.3 bis(3-methyl-5-tert.butyl-                                                                    171° C.                                                4-hydroxybenzyl)malonic                                                       acid-bis(2,2,6,6-tetra-                                                       methyl-4-piperidinyl)                                                         ester                                                  4    O        t-C.sub.4 H.sub.9                                                                      bis(3,5-di-tert.butyl-4-                                                                      225° C.                                                hydroxybenzyl)malonic                                                         acid-bis(2,2,6,6-tetra-                                                       methyl-4-piperidinyl-1-                                                       oxyl)ester                                             5    H        t-C.sub.4 H.sub.9                                                                      bis(3,5-di-tert.butyl-4-                                                                      205° C.                                                hydroxybenzyl)malonic                                                         acid-bis(2,2,6,6-tetra-                                                       methyl-4-piperidinyl)                                                         ester                                                  ______________________________________                                    

EXAMPLE 6

26 g (0.068 mole) of bis-(2,2,6,6-tetramethyl-4-piperidinyl) malonateand 17.8 g (0.068 mole) ofN-(3,5-di-tert.butyl-4-hydroxybenzyl)dimethylamine are dissolved in 200ml of toluene. After the addition of 0.5 g of lithium amide, the mixtureis refluxed for 3 hours. After cooling, the mixture is neutralised with1.5 ml of 1% acetic acid, and the organic phase repeatedly washed withwater. After drying over Na₂ SO₄, the solution is concentrated in vacuoto obtain, as oily residue, 3,5-di-tert.butyl-4-hydroxybenzyl-malonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester.

EXAMPLES 7 to 11

The products described in Table 2 are obtained analogously to Example 5,the procedure in this case being that in each test a malonic acidderivative of formula (III) is reacted with one mole of ahydroxybenzylamine of formula Va. ##STR13##

                  TABLE 2                                                         ______________________________________                                        Test                                                                          No.  X       Y       R.sub.3                                                                             Product       M.P.                                 ______________________________________                                        7    O       H       CH.sub.3                                                                            3-methyl-5-tert.                                                                            oily                                                            butyl-4-hydroxy-                                                                            residue                                                         benzylmalonic acid-                                                           bis(2,2,6,6-tetra-                                                            methyl-4-piperidi-                                                            nyl)ester                                          8    O       CH.sub.3                                                                              CH.sub.3                                                                            3-methyl-5-tert.                                                                            105°                                                     butyl-4-hydroxy-                                                              benzylmalonic acid-                                                           bis(1,2,2,6,6-pen-                                                            tamethyl-4-piperidi-                                                          nyl)ester.                                         9    O       CH.sub.3                                                                              t-C.sub.4 H.sub.9                                                                   3,5-di-tert.butyl-                                                                          oily                                                            hydroxybenzylmalonic                                                                        residue                                                         acid-bis(1,2,2,6,6-                                                           pentamethyl-4-piper-                                                          idinyl)ester                                       10   NH      H       t-C.sub.4 H.sub.9                                                                   3,5-di-tert.butyl-                                                                          253°                                                     4-hydroxybenzylmal-                                                           onic acid-bis(2,2,6,                                                          6-tetramethyl-4-pip-                                                          eridinyl)amide                                     11   NH      H       CH.sub.3                                                                            3-methyl-5-tert.                                                                            200°                                                     butyl-4-hydroxyben-                                                           zylmalonic acid-bis                                                           (2,2,6,6-tertamethyl-                                                         4-piperidinyl)amide                                ______________________________________                                    

EXAMPLE 12

24.5 g (0.076 mole) of 3,5-di-isopropyl-4-hydroxybenzylmalonic aciddimethyl ester and 23.8 g (0.15 mole) of4-hydroxy-2,2,6,6-tetramethylpiperidine are dissolved in 40 ml ofxylene. An addition is made to the solution, heated to 125°-130°, of 0.2g of lithium amide, with stirring; the solution is subsequently refluxedfor 2 hours; it is then cooled to about 50°, and neutralised with 0.8 mlof 1% acetic acid; the organic phase is washed with water and dried overNa₂ SO₄. After concentration in vacuo, there is obtained, as residue,3,5-di-isopropyl-4-hydroxybenzylmalonicacid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester, M.P. 123°.

EXAMPLE 13

100 Parts of polypropylene (melting index 3.2 g/10 min., 230°/2160 g)are intensively mixed, in a shaking apparatus, with 0.2 parts of one ofthe additives listed in the following Table 3 for 10 minutes. Theresulting mixture is kneaded in a Brabender plastograph at 200° for 10minutes; the mixture thus obtained is subsequently pressed out in aplaten press, with 260° platen temperature, to obtain 1 mm thick sheets,from which are stamped strips 1 cm in width and 17 cm in length.

The testing of the effectiveness of the additives incorporated in thetest strips is performed by heat ageing in an air-circulation furnace at135° and 149°, with an additive-free test strip serving as a comparison.Three test strips are used from each formulation. The final point isdefined as being that at which there commences an easily visiblecrumbling of the test strip.

                  TABLE 3                                                         ______________________________________                                        Stabiliser   Days to commencement of decomposition                            Ex. No.     149°   135°                                         ______________________________________                                        none         1             3                                                  1           34            140                                                 2           24            37                                                  3           21            86                                                  5           20            68                                                  8           17            48                                                  ______________________________________                                    

EXAMPLE 14

100 Parts of polypropylene (melting index 3.2 g/10 min., 230°/2160 g)are intensively mixed, in a shaking apparatus, with 0.1 part of one ofthe additives listed in the following Table 4 and 0.3 part ofdilaurylthiopropionate for 10 minutes. The resulting mixture is kneadedin a Brabender plastograph at 200° for 10 minutes: the mixture thusobtained is subsequently pressed out in a platen press, with 260° platentemperature, to produce 1 mm thick sheets, from which are stamped strips1 cm in width and 17 cm in length.

The testing of the effectiveness of the additives incorporated in thetest strips is performed by heat ageing in an air-circulation furnace at135° and 149°, whereby a test strip containing just the 0.3 part ofdilaurylthiodipropionate is taken as a comparison. Three test strips areused from each formulation. The final point is defined as being that atwhich there commences an easily visible decomposition of the test strip.

                  Table 4                                                         ______________________________________                                        Stabiliser   Days to commencement of decomposition                            Example No.  149°                                                                            135°                                             ______________________________________                                        Comparison    5        11                                                     1            56       130                                                     2            48       110                                                     3            37        86                                                     ______________________________________                                    

EXAMPLE 15

The specimens described in Example 13 were tested also with respect totheir colour stability as follows:

(a) after incorporation (Table 5, col. 2),

(b) after 500 hours exposure in a Xenotest apparatus of the film Hanau(Table 5, col. 3), and

(c) after 1-week's treatment with boiling water (Table 5, col. 4).

There was used for Table 5 an empirical colour scale in which 5 denotescolourlessness, 4 a barely perceptible slight discolouration, and 3, 2and 1 denote a successively greater discolouration.

                  Table 5                                                         ______________________________________                                                 Colour assessment according to the                                            Scale 1-5                                                            Stabiliser after incor-                                                                             after      boiling water                                Example No.                                                                              poration   exposure   1 week                                       ______________________________________                                        1          5          5          4-5                                          2          5          5          5                                            3          5          5          4-5                                          ______________________________________                                    

EXAMPLE 16

100 Parts of polypropylene (melting index 19 g/10 min., 230°/2160 g) areintensively mixed for 10 minutes, in a shaking apparatus, with 0.1 partof one of the stabilisers obtained according to Example 4 or Example 6.

The resulting mixture is extruded in a laboratory single screw extruder("Plamvo") at 260° nozzle temperature, 100 r.p.m. and a throughput of 50g/min, and subsequently granulated. The resulting granulate is spun in aspinning apparatus, with a nozzle temperature of 280°, intopolyfilaments, which are then stretched in the ratio of 1:5.5. Thesefilaments are subjected to a gas-fading test analogously to the AATCCStandard 23-1957, the test consisting in the exposure of the specimensto the exhaust gases of a butane-gas burner at 60° for 24 hours.

A visual assessment of colouration shows in both cases that thespecimens have remained colourless.

EXAMPLE 17

From the 1 mm thick test sheets described in Example 13 are cut, withthe aid of a Mikrotom, chips (clippings) having a thickness of 25μ.These clippings are clamped between pieces of stainless-steel mesh, andthe thus formed carriers then suspended in an air-circulation furnaceand aged at 135° and 147°, respectively. The end point is defined asbeing the time after which, with slight tapping of the mesh containers,decomposed polypropylene falls out in powder form (control 1--2× daily).The results are given in hours (Table 6).

                  TABLE 6                                                         ______________________________________                                        Stabiliser   Hours to commencement of decomposition                           Example No.  at 147°                                                                              at 135°                                     ______________________________________                                        without      10             20                                                additive                                                                      1            120           280                                                2            70            210                                                3            45            140                                                ______________________________________                                    

EXAMPLE 18

Chips (clippings) 25μ thick are cut, with the aid of a Mikrotom, fromthe 1 mm thick test sheets described in Example 14. These clippings areclamped between pieces of stainless-steel mesh, and the thus formedcarriers then suspended in an air-circulation furnace and aged at 135°and 147°, respectively. The end point is defined as being the time atwhich, on slight tapping of the mesh containers, decomposedpolypropylene falls out in powder form (control 1--2× daily). Theresults are given in hours (Table 7).

                  TABLE 7                                                         ______________________________________                                        Stabiliser  Hours to commencement of decomposition                            Example No. at 147°                                                                              at 135°                                      ______________________________________                                        Comparison   10            20                                                 1           120           280                                                 2           140           285                                                 3           120           280                                                 ______________________________________                                    

EXAMPLE 19

100 Parts of polypropylene powder (Moplen Fibre grade, of the firmMontedison) with 0.2 parts of β-(3,5-ditert.butyl-4-hydroxyphenyl)propionic acid octadecyl ester and 0.25 part of astabiliser from the following Table 8 are homogenised in a Brabenderplastograph at 200° C. for 10 minutes. The resulting mixture is removedas quickly as possible from the kneader, and moulded in a toggle pressinto the form of 2-3 mm thick sheet. A portion of the moulded sheet thusobtained is cut out and then pressed out between two high-gloss hardaluminum sheets under a hand-hydraulic laboratory press for 6 minutes at260° with a pressure of 12 tons to give a sheet 0.5 mm in thickness,which is immediately quenched in cold water. From this 0.5 mm sheet isthen prepared, under exactly the same conditions, the 0.1 mm thick testsheet material. Specimens each 60×44 mm in size are stamped out fromthis material and irradiated in the Xenotest 150. These specimens areremoved at regular intervals of time from the exposure apparatus andtheir carbonyl content measured in an IR-spectrophotometer. The increaseof the carbonyl extinction on exposure to light is a measure for thephotooxidative decomposition of the polymer [cp. L. Balaban et al., JPolymer Sci. Part C, 22, 1059-1071 (1969); J. F. Heacock, J. PolymerSci. Part A-1, 22, 2921-34 (1969); D. J. Carlsson and D. M. Wiles,Macromolecules 2, 587-606 (1969)] and, as known from experience, isassociated with a decline of the mechanical properties of the polymer.Thus, for example, the comparison sheet (stabilised only withantioxidant) is completely brittle on attainment of a carbonylextinction of ca. 0.300.

The protective action of the stabilisers according to the invention isclearly shown by the following Table 8.

                  Table 8                                                         ______________________________________                                        Stabiliser                  CO-Extinction                                     Example No.                                                                            Exposure time in hours                                                                           (5.85 μ)                                       ______________________________________                                        Comparison                                                                              800               0.30                                              1        >6000              0.010                                             2        >6000              0.010                                             7        >5000              0.010                                             10       >5000              0.010                                             ______________________________________                                    

EXAMPLE 20

100 Parts of polystyrene granules are mixed dry with 0.25 parts of astabiliser from the following Table 9; the mixture is then re-granulatedin an extruder, and subsequently processed, in an injection-mouldingmachine, into the form of sheets 2 mm in thickness. The sheets thusobtained are afterwards irradiated for 2000 hours in a Xenotestapparatus 150, and their yellowing values determined by means of theyellowing factor in the following manner: ##EQU1## whereby ΔT denotesthe transmission loss with the wave lengths 420 and 680 nm duringexposure of the specimens, and T (560) is the transmission value as apercentage of the value in the case of the unexposed speciment at 560nm.

                  Table 9                                                         ______________________________________                                                      Example                                                         Stabiliser    No.      Y.F.                                                   No stabiliser      20.0                                                       ______________________________________                                        1                  4.5                                                        6                  5.5                                                        ______________________________________                                    

We claim:
 1. A composition of matter comprising an organic polymernormally subject to degradation by oxidation, light or heat, and as astabilizer from 0.01 to 5% of at least one compound of the formula##STR14## wherein X can be oxygen or --NH--,Y represents hydrogen, theradical --O., an alkyl group having 1 to 12 carbon atoms, an alkenylgroup having 3 or 4 carbon atoms, a propargyl group, a benzyl group, ora group of the formula ##STR15## wherein R₆ represents hydrogen, methylor phenyl, and R₇ represents hydrogen, or an acyl group selected fromthe group consisting of acetyl, propionyl, hexanoyl, acryl, methacryl,2-ethylhexanoyl, dodecanoyl, octadecanoyl and benzoyl, R₁ represents ahydroxybenzyl group of formula (II) ##STR16## wherein R₃ and R₄ eachindependently represent an alkyl group having 1 to 8 carbon atoms, andR₅ represents hydrogen or methyl, and R₂ represents, if X is oxygen,hydrogen, or a hydroxybenzyl group of formula (II); if however, X is--NH--, only hydrogen.
 2. A composition of claim 1 whereinY representshydrogen, the radical --O., methyl, allyl or benzyl group, and R₁represents a hydroxybenzyl group of the formula ##STR17## wherein R₃represents isopropyl, tert.butyl or tert.amyl group, R₄ representsmethyl, ethyl, isopropyl, tert.butyl, tert.amyl or tert.octyl group, andR₅ represents hydrogen or methyl.
 3. A composition of claim 1 whereinYrepresents hydrogen, the radical --O. or methyl group, R₃ representstert.butyl group, R₄ represents methyl or tert.butyl group, and R₅represents hydrogen.
 4. A composition of matter according to claim 1,where the polymer is a polyolefin.
 5. A composition of claim 1 whereinYrepresents hydrogen, the radical --O. or methyl group, and R₁ representsa hydroxybenzyl group of formula (IIb) ##STR18## wherein R₃ representstert.butyl, tert.amyl or tert.octyl group.
 6. A composition of claim 4stabilized with bis(2,2,6,6-tetramethyl-4-piperidinyl) ester ofbis(3,5-di-tert.butyl-4-hydroxybenzyl)malonic acid.
 7. A composition ofclaim 4 stabilized with bis(1,2,2,6,6-pentamethyl-4-piperidinyl) esterof bis(3-methyl-5-tert.butyl-4-hydroxybenzyl)malonic acid.
 8. Acomposition of claim 4 stabilized withbis(1,2,2,6,6-pentamethyl-4-piperidinyl) ester ofbis(3,5-di-tert.butyl-4-hydroxybenzyl)malonic acid.
 9. A composition ofclaim 4 stabilized with bis(2,2,6,6-tetramethyl-4-piperidinyl) ester of3-methyl-5-tert.butyl-4-hydroxybenzylmalonic acid.
 10. Method forstabilizing organic polymers against thermal oxidative and light-inducedageing by adding to the polymer 0.01 to 5 percent by weight of at leastone compound of formula (I) ##STR19## wherein X can be oxygen or--NH--,Y represents hydrogen, the radical --O., an alkyl group having 1to 12 carbon atoms, an alkenyl group having 3 or 4 carbon atoms, apropargyl group, a benzyl group, or a group of the formula ##STR20##wherein R₆ represents hydrogen, methyl or phenyl, and R₇ representshydrogen, or an acyl group selected from the group consisting of acetyl,propionyl, hexanoyl, acryl, methacryl, 2-ethyl-hexanoyl, dodecanoyl,octadecanoyl and benzoyl, R₁ represents a hydroxybenzyl group of formula(II) ##STR21## wherein R₃ and R₄ each independently represent an alkylgroup having 1 to 8 carbon atoms, and R₅ represents hydrogen or methyl,and R₂ represents, if X is oxygen, hydrogen, or a hydroxybenzyl group offormula (II); if, however, X is --NH--, only hydrogen.
 11. Methodaccording to claim 10, wherein the polymer is a polyolefin.